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Hello,

My Dad who is 75 and diagnosed with PD for 4 years has had sleep apnea as
long as I can remember. This past year, he stayed at the VA sleep clinic
here in Little Rock, Arkansas on two separate occasions.

He was "officially" diagnosed with sleep apnea as a result, but has declined
to wear the positive air apparatus for sleeping.

Although no physician has ever said this, it in my opinion, 40 to 50 years
of being oxygen deprived hundreds of time during the night can't be good for
one's brain, but nobody can or will address that it seems (probably because
there is not enough info substantiated about apnea). When he had a MRI about
three years ago, his was shot full of tiny white spots which no one would
venture an opinion to their origin and although I come across the term Lewy
bodies here and there in the PD literature I don't know what they are
really. All that was said about the white spots was that all of us acquire a
few each year as we age but my Dad had an enormous amount (this comment from
his movement specialist).

In 1990, my Dad was a participant in a nation wide sleep study during which
he spent five days being hooked up to many sleep monitoring devices.
However, that study's protocol was looking at the effects of two alcoholic
drinks ingested right before sleep. After completing the five nights, there
was never a mention of sleep apnea although I know they couldn't have missed
it with all the monitoring equipment on him. Then again, they might have
mentioned it to him at the time and he declined to tell me since I tend to
take things too seriously (he thinks) as far as he is concerned. Hopefully,
documenting and addressing his apnea twelve years ago wouldn't have had any
positive effect on the course of his PD symptoms but no one will ever know.
When I think otherwise, I get a little angry, even though I realize that
that studies are concerned with one thing, and one thing only (at least this
is what I tell myself).Trying not to think thoughts of what might have been
. . .

CGJann

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